OrphanDrug
OrphanDrug
Pharma Knowledge Base

familial multinodular goiter

MeSH: C562732ORPHA: 276399

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Clinical Presentation
  4. 4. Classification & Codes

Overview

instance of multinodular goiter that is caused by an inherited modification of the individual's genome

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Clinical Presentation

Signs and symptoms associated with familial multinodular goiter, sourced from HPO and Orphanet clinical annotations.

Multinodular goiterBasal cell carcinomaRenal cell carcinomaPleuropulmonary blastomaOvarian neoplasmTesticular seminomaSertoli cell neoplasmColorectal polyposisThyroid carcinomaAlveolar rhabdomyosarcomaCerebellar medulloblastomaMedulloepitheliomaPilomatrixoma

Classification & Codes

MeSH Code

C562732

Orphanet Code

ORPHA:276399
familial multinodular goiter
MeSHC562732
OrphanetORPHA:276399
Treatments0 drug(s)
Symptoms on record13 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO